Canonical Allele Identifier: CA297648
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181766
dbSNP Id: rs535800148

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112477951G>A , CM000674.2:g.112477951G>A GRCh38
NC_000012.11:g.112915755G>A , CM000674.1:g.112915755G>A GRCh37
NC_000012.10:g.111400138G>A NCBI36
NG_007459.1:g.64220G>A , LRG_614:g.64220G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000639857.2:c.1028G>A ENSP00000491593.2:p.Arg343Gln
ENST00000685487.1:c.1028G>A ENSP00000508503.1:p.Arg343Gln
ENST00000687906.1:c.914G>A ENSP00000509536.1:p.Arg305Gln
ENST00000688597.1:c.1028G>A ENSP00000510628.1:p.Arg343Gln
ENST00000690210.1:c.1028G>A ENSP00000509272.1:p.Arg343Gln
ENST00000692624.1:c.1028G>A ENSP00000508953.1:p.Arg343Gln
ENST00000351677.7:c.1028G>A MANE Select ENSP00000340944.3:p.Arg343Gln
ENST00000351677.6:c.1028G>A ENSP00000340944.2:p.Arg343Gln
ENST00000392597.5:c.1028G>A ENSP00000376376.1:p.Arg343Gln
ENST00000635625.1:c.1028G>A ENSP00000489597.1:p.Arg343Gln
ENST00000635652.1:c.20G>A ENSP00000489541.1:p.Arg7Gln
NM_002834.3:c.1028G>A , LRG_614t1:c.1028G>A NP_002825.3:p.Arg343Gln
NM_080601.1:c.1028G>A NP_542168.1:p.Arg343Gln
XM_006719526.1:c.1028G>A XP_006719589.1:p.Arg343Gln
XM_006719527.1:c.914G>A XP_006719590.1:p.Arg305Gln
XM_011538613.1:c.1025G>A XP_011536915.1:p.Arg342Gln
NM_001330437.1:c.1028G>A NP_001317366.1:p.Arg343Gln
NM_002834.4:c.1028G>A NP_002825.3:p.Arg343Gln
NM_080601.2:c.1028G>A NP_542168.1:p.Arg343Gln
XM_011538613.2:c.1025G>A XP_011536915.1:p.Arg342Gln
XM_017019722.1:c.1025G>A XP_016875211.1:p.Arg342Gln
NM_001330437.2:c.1028G>A NP_001317366.1:p.Arg343Gln
NM_001374625.1:c.1025G>A NP_001361554.1:p.Arg342Gln
NM_002834.5:c.1028G>A MANE Select NP_002825.3:p.Arg343Gln
NM_080601.3:c.1028G>A NP_542168.1:p.Arg343Gln